Product Recalls in Montana

Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,101 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,101 in last 12 months

Showing 2341–2360 of 27,852 recalls

Medical DeviceDecember 20, 2024· Max Mobility LLC

Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...

The Issue: Due to faulty circuit board in speed control remote use in conjunction with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Randox Laboratories, Limited

Recalled Item: Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Recalled by Randox...

The Issue: Lipoprotein (a) on Roche Cobas c501 with nmol/l claims does not have a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Delivery System 10mmx10mm UPN: M00553740 Recalled by Boston...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Breathe Technologies Recalled by Baxter Healthcare Corporation Due to There...

The Issue: There is an issue with the ventilator battery charger that could lead to an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Ortho-Clinical Diagnostics, INc.

Recalled Item: Brand Name: VITROS Product Name: VITROS XT 7600 Integrated System Recalled...

The Issue: The VITROS XT 7600 Integrated System software versions 3.8.0 may not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Ortho-Clinical Diagnostics, INc.

Recalled Item: Brand Name: VITROS Product Name: VITROS 3600 Immunodiagnostic System...

The Issue: The VITROS 3600 Immunodiagnostic System software versions 3.8.0 may not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Jinan Bodor Cnc Machine Co Ltd

Recalled Item: Bodor P and C series laser cutting machines Recalled by Jinan Bodor Cnc...

The Issue: Non-compliant laser products

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope - - Optical Biopsy and Grasping Forceps Recalled by...

The Issue: Due to failure of manual cleaning validation, biopsy and grasping forceps...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Due to an increase in...

The Issue: Due to an increase in complaints for pitch cable failures related to forceps...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Due to an increase in...

The Issue: Due to an increase in complaints for pitch cable failures related to forceps...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· New Medical Technologies Gmbh

Recalled Item: Integra Miltex Cryosolutions Cartridges 4 Pack (23.5g N2O each) Recalled by...

The Issue: During the assembly of the cartridge to its connecting body part, the valve...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· New Medical Technologies Gmbh

Recalled Item: Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each) Recalled by...

The Issue: During the assembly of the cartridge to its connecting body part, the valve...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing